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A Wehnert

Showing results (11-20 of 26) with videos related to

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Human Genetics|January 1, 1988
The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1P Raeymaekers, C Van Broeckhoven, H Backhovens, et al.
Nature Genetics|May 1, 1994
Apolipoprotein E4 allele in a population-based study of early-onset Alzheimer's diseaseC M van Duijn, P de Knijff, M Cruts, et al.
Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
American Journal of Human Genetics|October 1, 1994
A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21C M van Duijn, L Hendriks, L A Farrer, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 24, 1999
Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNAJ Theuns, M Cruts, J Del-Favero, et al.
Annals of Neurology|May 1, 1995
The apolipoprotein E epsilon 2 allele is associated with an increased risk of early-onset Alzheimer's disease and a reduced survivalC M van Duijn, P de Knijff, A Wehnert, et al.
Nature|September 10, 1987
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European familiesC Van Broeckhoven, A M Genthe, A Vandenberghe, et al.
Science (New York, N.Y.)|June 1, 1990
Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)C Van Broeckhoven, J Haan, E Bakker, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphismsP Stinissen, B Van Roy, G Van Camp, et al.
Neurology|June 1, 1989
Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markersP Raeymaekers, P De Jonghe, H Backhovens, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Human Genetics|January 1, 1988
The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1P Raeymaekers, C Van Broeckhoven, H Backhovens, et al.
Nature Genetics|May 1, 1994
Apolipoprotein E4 allele in a population-based study of early-onset Alzheimer's diseaseC M van Duijn, P de Knijff, M Cruts, et al.
Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
American Journal of Human Genetics|October 1, 1994
A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21C M van Duijn, L Hendriks, L A Farrer, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 24, 1999
Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNAJ Theuns, M Cruts, J Del-Favero, et al.
Annals of Neurology|May 1, 1995
The apolipoprotein E epsilon 2 allele is associated with an increased risk of early-onset Alzheimer's disease and a reduced survivalC M van Duijn, P de Knijff, A Wehnert, et al.
Nature|September 10, 1987
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European familiesC Van Broeckhoven, A M Genthe, A Vandenberghe, et al.
Science (New York, N.Y.)|June 1, 1990
Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)C Van Broeckhoven, J Haan, E Bakker, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphismsP Stinissen, B Van Roy, G Van Camp, et al.
Neurology|June 1, 1989
Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markersP Raeymaekers, P De Jonghe, H Backhovens, et al.
Pageof 3